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Bigger Isn't Always Better: Cell Size and the Spindle Assembly Checkpoint
Abigail R Gerhold1, Jean-Claude Labbé2, Paul S Maddox3
1Institute of Research in Immunology and Cancer (IRIC), Université de Montréal, C.P. 6128, Succursale Centre-ville, Montréal, QC H3C 3J7, Canada.
Developmental Cell
|February 10, 2016
Summary
Spindle assembly checkpoint activity varies between cell types. This study reveals checkpoint activity increases during development as cell size and the cytoplasm-to-kinetochore ratio decrease.
Area of Science:
- Cell biology
- Developmental biology
- Genetics
Background:
- The spindle assembly checkpoint (SAC) ensures proper chromosome segregation during cell division.
- Variability in SAC activity across different cell types is known but not well understood.
Purpose of the Study:
- To investigate the factors contributing to the observed variability in spindle assembly checkpoint activity.
- To understand how SAC regulation changes during cellular development.
Main Methods:
- Analysis of spindle assembly checkpoint activity in various cell types.
- Correlation of checkpoint activity with cell size and cytoplasm-to-kinetochore ratio during development.
Main Results:
- Spindle assembly checkpoint activity was found to increase during the developmental process.
- This increase in checkpoint activity inversely correlates with decreasing cell size.
- A decreasing cytoplasm-to-kinetochore ratio also correlates with enhanced checkpoint activity.
Conclusions:
- Cell size and the cytoplasm-to-kinetochore ratio are key regulators of spindle assembly checkpoint activity.
- Developmental changes in cell physiology directly impact the efficacy of the spindle assembly checkpoint.
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